Head of Manufacturing Science & Technology (MST)
Department: MST
Reports to: CEO
Direct Reports: MST Scientist
Location: Oklahoma city, OK
About the Role
We are seeking a highly experienced and strategic leader to head the Manufacturing Science & Technology (MST) function. This individual will drive process innovation, ensure smooth production support, and align MST activities with business and regulatory objectives. The Head of MST will play a critical role in overseeing process technologies, resolving technical challenges, and leading technology transfer and scale-up initiatives to strengthen operational excellence.
Key Responsibilities
Develop and execute annual MST plans aligned with corporate strategy and operational goals.
Lead the MST team in providing technical support to production, ensuring compliance and efficient execution of activities.
Supervise and guide process development and optimization to enhance efficiency, robustness, and compliance.
Troubleshoot and resolve production-related technical issues, maintaining process stability.
Drive technology transfer and scale-up initiatives to ensure reproducibility and reliability of processes.
Support internal and external audits/inspections to ensure GMP and regulatory compliance.
Establish, implement, and continuously improve laboratory systems, SOPs, and quality standards.
Mentor, train, and develop the MST team to build technical capability and organizational strength.
Minimum Qualifications
Master’s degree or higher in Biotechnology, Pharmaceuticals, Chemical Engineering, or related discipline.
10+ years of relevant experience in the biopharmaceutical industry, with at least 5 years in team leadership roles.
Proven expertise in large molecule drug development, technology transfer, process optimization, and GMP compliance. PEPTIDES AND GLP-1
Strong leadership skills with the ability to build, develop, and retain high-performing teams.
Excellent problem-solving, communication, and cross-functional collaboration skills.
Fluent in English (written and verbal).
Preferred Qualifications
Prior experience in a CDMO environment.
Familiarity with U.S. FDA and EU regulatory requirements.